Senior statistical programmer - 12 month contract

We are looking for a highly experienced Clinical Statistical Programmer to independently lead programming activities across clinical studies. This role requires deep expertise in SDTM and ADa M dataset development, complex TLF generation, and regulatory submission support.
Key Responsibilities
Design, develop, and validate SAS programs for SDTM, ADa M, and TLF outputs
Produce submission-ready datasets and documentation, including Define.xml
Review and interpret SAPs and data management plans to determine programming requirements
Ensure deliverables comply with CDISC and regulatory standards
Lead programming activities for assigned studies with minimal supervision
Collaborate with cross-functional teams and external vendors on data standards and transfers
Perform quality control and validation of datasets and outputs
Identify and implement process improvements to enhance efficiency and consistency
Contribute to continuous improvement initiatives ...